In this study, we investigate the structural and dynamical characteristics of the biopolymer pectin, exploring its impact on ion transport, diffusion activation energy, and relaxation timescales within a saltwater environment (100 mM NaCl (aq.)) using classical molecular dynamics (MD) simulations. Our analysis of radial distribution functions (g(r)) reveals a notable preference of Na+ ions to interact more extensively with pectin compared to Cl- ions. Moreover, we observe slight variations in the strength of inter-ion interactions, with a modest decrease in ion-pectin interaction strength with increased pectin loading. Additionally, our findings indicate that sodium exhibits the lowest diffusion coefficient due to the presence of significant energy barriers among Na+, Cl-, and water molecules, following the sequence: D(water) > D(Cl-) > D(Na+) at any pectin loading and temperature conditions within pectin-saltwater membranes. Furthermore, our study demonstrates that viscosity, ion-pair relaxation timescales and ion-cage relaxation timescales exhibit monotonic increases with pectin loading while displaying the opposite trend with temperature. Overall, our simulations strongly endorse the use of biopolymer pectin as a highly promising and innovative option for a wide range of industrial applications, including flexible hydrogel electrolytes and saline water treatment.